Muñoz-Serrano Antonio J, Ramírez-Amoros Carla, Barrena Delfa Saturnino, Oterino César, Navarro Gema, Rubio Aparicio Pedro, Pérez-Martínez Antonio, Martínez-Urrutia María José, Martínez Leopoldo
Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain.
Department of Pediatric Radiology, Hospital Universitario La Paz, Madrid, Spain.
Pediatr Blood Cancer. 2025 Aug;72(8):e31828. doi: 10.1002/pbc.31828. Epub 2025 May 27.
Sarcopenia (SP) is described as a prognostic factor in adult and pediatric cancer patients. However, there are no data regarding Wilms tumor (WT). We aimed to study the association between sarcopenia and oncological outcomes in WT.
A retrospective study of patients diagnosed with WT at our institution between 2010 and 2022 was performed. SP at diagnosis was assessed by measuring the psoas muscle area (PMA) at the L4-L5 level on computed tomography (CT)/magnetic resonance imaging (MRI), and was defined as z-score values ≤2. Demographics, complications, and outcomes were analyzed.
Forty-eight patients (50% male) were included, with a mean age of 44.91 ± 31.12 months. Twelve patients (25%) had SP at diagnosis versus 36 (75%) who did not. Forty-one patients (85%) underwent total nephrectomy and seven (15%) nephron-sparing surgery (NSS). No statistical differences were found in demographics, risk group, or treatment between the SP and non-sarcopenic (NSP) groups. SP was associated with a higher rate of postsurgical complications (33% for the SP-group vs. 5.6% for the NSP-group; p = 0.023) and with a higher rate of relapse (33% vs. 14%, respectively; p = 0.09). With a median follow-up of 57.75 (1.87-150.8) months, event-free survival (EFS) was lower for the SP group (84.20 ± 17.45 vs. 135.40 ± 8.65 months, respectively; p = 0,08). One patient in the SP group died. The 5-year overall survival (OS) was 89% for the SP group versus 100% for the NSP group.
Among our patients, SP can be considered a risk factor for complications in patients with WT and could be associated with poor outcomes, increasing the risk of relapse and decreasing EFS.
肌肉减少症(SP)被认为是成人和儿童癌症患者的一个预后因素。然而,关于肾母细胞瘤(WT)的数据尚不存在。我们旨在研究WT中肌肉减少症与肿瘤学结局之间的关联。
对2010年至2022年期间在我们机构被诊断为WT的患者进行了一项回顾性研究。通过在计算机断层扫描(CT)/磁共振成像(MRI)上测量L4-L5水平的腰大肌面积(PMA)来评估诊断时的SP,并将其定义为z评分值≤2。分析了人口统计学、并发症和结局。
纳入48例患者(50%为男性),平均年龄为44.91±31.12个月。12例患者(25%)在诊断时有SP,36例(75%)没有。41例患者(85%)接受了全肾切除术,7例(15%)接受了保肾手术(NSS)。SP组和非肌肉减少症(NSP)组在人口统计学、风险组或治疗方面未发现统计学差异。SP与术后并发症发生率较高相关(SP组为33%,NSP组为5.6%;p=0.023),且复发率较高(分别为33%和14%;p=0.09)。中位随访57.75(1.87-150.8)个月,SP组的无事件生存期(EFS)较低(分别为84.20±17.45个月和135.40±8.65个月;p=0.08)。SP组有1例患者死亡。SP组的5年总生存率(OS)为89%,NSP组为100%。
在我们的患者中,SP可被视为WT患者发生并发症的一个危险因素,并且可能与不良结局相关,增加复发风险并降低EFS。